I just had a sleep study and the results are:
ALPHA INTRUSION INTO DELTA SLEEP this means that 'awake' brainwaves (alpha waves) are firing during delta (deep) sleep.
I also had REDUCED REM AND DEEP SLEEP

Both of these result in non restorative sleep.

Anyone know more about this or Does anyone know if this is common in MS??
I also have seizures and severe migraines.

I have no advice or knowledge on this. just wanted to hug you I am facinated and want to know more tho.

Thanks for sharing that, Daisy. It is a mystery to me, what causes our sleep or "not to sleep" patterns.

I'm sure that MS, which causes lesions on our brain, can certainly cause our sleeping hours to be interupted, just as it does to our waking hours.

What is the solution, is the question?? Some life threatening sleep patterns like sleep apnea, when you quit breathing during sleep, must have a solution, such as a CRAPS mask. (My young nephew (35) died in his sleep from SA.)

I am so sorry about your migraines and seisures. I hope you can find the right med to control this.

Let us know how you are doing and take care of yourself...

I do not have apnea...thank God.

I do not have a follow up until Nov 9th.....but from what I have read, this sleep distrubance is a common occurance in patients with chronic pain and/or fibromyalgia. The only treatment to date is GHB, the 'date rape' drug....which is legal now under the drug name XYREM. But it comes with potential serious side effects.

Also in my reading, I have found that MS patients have a higher occurance of sleep disorders.

Hi Daisy - I chart my sleep patterns daily as it clearly shows the progression of a flare up for me.

I begin with sleeping normally from 10pm to 5/6am. Slowly the pattern will start to change.

It begins with not being able to sleep for more than 3-4 hours. Ex. I go to bed at 10pm but awaken at 12:30 to 2am. Then I can not get back to sleep.
Naps start to increase from once a day to twice a day. Length of naps start to increase.

I'm in full swing of a flare up headed to the peak of fatigue which can take about 4-6 weeks to get to the peak - new symptom arrives - and then I start heading down towards normal life style again.

At my peak I sleep almost 18-20 hours a day barely struggling through the 4 hours of awakeness.

Keeping the daily journal visually, helps me stay hopeful and encouraging as I can watch the progression and then see when it starts to decline-aw sweet relief is on the way as my fatigue begins to decline and I start to awaken to life again.

The more clearly you can follow or understand how this disease affects your body system can help ease anxiety/depression etc.

For me it helped keep depression, sadness etc away because I could "see" and "know" how my days were being numbered. Like a menstrual period...each woman is different and you have to know your body and how this disease affects your body system.

I really wish I could 'chart' mine.....To me, it seems to have no rhyme or reason.....or I am just too pre-occupied to see the pattern.